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1 MHz probe, monitoring

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 6025-1Model Monitoring Probes

by Compumedics Germany GmbH

Identity

Trade Name
1 MHz Probe, click&stay, right side, green labeling EUDAMED
1 MHz probe, monitoring FDA UDI
Generic Name
Noninvasive vascular ultrasound system probe FDA UDI
Device Name
1 MHz Probes, click&stay, left side, orange labeling EUDAMED
1 MHz probe (2.5 meter cable), click & stay, monitoring, green marking FDA UDI
Model / Reference
Monitoring Probes EUDAMED
6025-1 EUDAMED
1 MHz_M_C&S_g FDA UDI
Description
1 MHz probe (2.5 meter cable), click & stay, monitoring, green marking FDA UDI

Identifiers

Catalog Number
6025 FDA UDI
Primary DI / UDI-DI
04260493310260 EUDAMEDFDA UDI
Basic UDI-DI
4260493316016VE EUDAMED
Direct Marketing DI
04260493310260 EUDAMED
510(k) Number
K051085 FDA UDI
FDA Product Code
ITX FDA UDI
EMDN Code
Z11040299 ULTRASOUND PROBES – OTHER EUDAMED
GMDN Term
Noninvasive vascular ultrasound system probe FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
892.1570 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Noninvasive vascular ultrasound system probe

1 MHz probe, monitoring by Compumedics Germany GmbH — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Noninvasive vascular ultrasound system probe.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 1b5517f2-196f-4f52-9ae9-e6c958fce60d 36 fields · synced Jul 13, 2026
  • EUDAMED c17a3d70-49a9-4260-9b36-6bdb9aa1ab5f 61 fields · synced Jul 13, 2026